Primary Site >> Liver Cancer

Gene >> LRP4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000378623
Start 46875070:46875070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3959G>A
AA Mutation p.Cys1320Tyr(p.C1320Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000378623
Start 46899935:46899935(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.358G>A
AA Mutation p.Gly120Ser(p.G120S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000378623
Start 46890472:46890472(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1720G>A
AA Mutation p.Gly574Ser(p.G574S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000378623
Start 46875639:46875639(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3742T>A
AA Mutation p.Leu1248Met(p.L1248M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000378623
Start 46900288:46900288(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.290A>T
AA Mutation p.Glu97Val(p.E97V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000378623
Start 46874892:46874892(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4137C>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000378623
Start 46859270:46859270(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5431G>T
AA Mutation p.Glu1811Ter(p.E1811*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript